Changes in the incidence and etiology of congenital hypothyroidism detected during 30 years of a screening program in central Serbia-Reference-Cited by-同舟云学术

Changes in the incidence and etiology of congenital hypothyroidism detected during 30 years of a screening program in central Serbia

Published:2015-09-07 Issue:2 Volume:175 Page:253-259
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Mitrovic Katarina^ORCID,Vukovic Rade,Milenkovic Tatjana,Todorovic Sladjana,Radivojcevic Jovana,Zdravkovic Dragan

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00431-015-2630-5.pdf

Reference18 articles.

1. Albert BB, Cutfield WS, Webster D, Carll J, Derraik JGB, Jefferies C, Gunn AJ, Hofman PL (2012) Etiology of increasing incidence of congenital hypothyroidism in New Zealand from 1993–2010. J Clin Endocrinol Metab 97:3155–3160

2. Banicevic M, Subotic Z, Kurt N (1987) Clinical and laboratory characteristics of congenital hypothyroidism in neonates detected in a screening program. Srp Arh Celok Lek 115:677–697

3. Botler J, Camacho LA, Cruz MM (2012) Phenylketonuria, congenital hypothyroidism and haemoglobinopathies: public health issues for Brazilian newborn screening program. Cad Saude Publica 28:1623–1631

4. Chiesa A, Prieto L, Mendez V, Papendieck P, De Lujan CM, Gruneiro-Papendieck L (2013) Prevalence and etiology of congenital hypothyroidism detected through an Argentine neonatal screening program (1997–2010). Horm Res Paediatr 80:185–192

5. Corbetta C, Weber G, Cortinovis F, Calebrio D, Passoni A, Vigone MC, Beck-Peccoz P, Chiumello G, Persani L (2009) A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH). Clin Endocrinol 71:739–745

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